|Número de publicación||US5069970 A|
|Tipo de publicación||Concesión|
|Número de solicitud||US 07/451,704|
|Fecha de publicación||3 Dic 1991|
|Fecha de presentación||18 Dic 1989|
|Fecha de prioridad||23 Ene 1989|
|Número de publicación||07451704, 451704, US 5069970 A, US 5069970A, US-A-5069970, US5069970 A, US5069970A|
|Inventores||Theodore Largman, Frank Mares, Clarke A. Rodman|
|Cesionario original||Allied-Signal Inc.|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (12), Citada por (350), Clasificaciones (16), Eventos legales (4)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
This application is a division of application Ser. No. 300,194, filed 1/23/89, now U.S. Pat. No. 4,908,052, which is a continuation of U.S. Ser. No. 040,446, filed 4/20/87.
1. Field of the Invention
This invention relates to improved filter fibers and filters comprising said fibers. More particularly, this invention relates to such filter fibers comprising a polyester and a polyolefin, and filters comprising said fibers.
2. Prior Art
Polyesters are well known materials for the manufacture of fibers. Illustrative of such fibers are those described in U.S. Pat. Nos. 4,454,196; 4,410,473; and 4,359,557.
Polyolefinic materials are well known articles of commerce which have experienced wide acceptance in forming shaped objects and film or sheet material. The use of such materials has extended to the fiber and fabric industries. For example, U.S. Pat. Nos. 4,587,154; 4,567,092; 4,562,869; and 4,559,862.
Fibers containing mixtures of polyolefins and polyesters are known. For example, U.S. Pat. No. 3,639,505 describes fibers and films composed of a polymer alloy comprising an intimate blend of polyolefin, a minor amount of polyethylene terephthalate and 0.2 to 5 parts per hundred parts of polymer of a toluene sulfonamide compound which are described as having improved receptivity to dispersed dyes.
Bicomponent fibers are known in the art. For example, Textile World, June 1986 at page 29 describes sheath/core fibers which have an inner core of polyester and have an outer core of polypropylene or polyethylene. Also see Textile World, April 1986, page 31.
Bicomponent textile filaments of polyester and nylon are known in the art, and are described in U.S. Pat. No. 3,489,641. According to the aforesaid patent, a yarn that crimps but does not split on heating is obtained by using a particular polyester.
It is also known to employ as the polyester component of the bicomponent filament a polyester which is free from antimony, it having been determined that antimony in the polyester reacts with nylon to form a deposit in the spinneret which produces a shorter junction line, and thus a weaker junction line. Such products are claimed in U.S. patent application Ser. No. 168,152, filed July 14, 1980.
It is also known to make bicomponent filaments using poly[ethylene terephthalate/5-(sodium sulfo) isophthalate] copolyester as the polyester component. U.S. Pat. No. 4,118,534 teaches such bicomponents.
It is also known to make bicomponent filaments in which the one component partially encapsulates the other component. U.S. Pat. No. 3,607,611 teaches such a bicomponent filament.
It is also known to produce bicomponent filaments in which the interfacial junction between the two polymeric components is at least in part jagged. U.S. Pat. No. 3,781,399 teaches such a bicomponent filament. Bicomponent filaments having a cross sectional dumbell shape are known in the art. U.S. Pat. No. 3,092,892 teaches such bicomponent filaments. Other nylon/polyester bicomponent fibers having a dumbell cross sectional shape having a jagged interfacial surface, the polyester being an antimony-free copolyester having 5-(sodium sulfo) isophthalate units are known. U.S. Pat. No. 4,439,487 teaches such fibers. The surface of such bicomponent filament is at least 75% of one of the polymeric components. Still other nylon/polyester bicomponent sheath/core fibers are described in Japan Patent Nos. 49020424, 48048721, 70036337 and 68022350; and U.S. Pat. Nos. 4,610,925, 4,457,974 and 4,610,928.
Fibers have previously been prepared from blends of polyamides with minor amounts of polyesters such as poly(ethylene terephthalate). Intimate mixing before and during the spinning process has been recognized as necessary to achieve good properties in such blended fibers. It is furthermore known that the fine dispersions in fibers of polymer blends are achieved when both phases have common characteristics such as melt viscosity. See D. R. Paul, "Fibers From Polymer Blends" in Polymer Blends, vol. 2, pp. 167-217 at 184 (D. R. Paul & S. Newman, ehs., Academic Press 1978)
Graft and block copolymers of nylon 6/nylon 66, nylon 6/poly(ethylene terephthalates) and nylon 6/poly(butylene terephthalate) have been formed into grafts which can be spun into fibers For example, U.S. Pat. No. 4,417,031, and S. Aharoni, Polymer Bulletin, vol. 10, pp. 210-214 (1983) disclose a process for preparing block and/or graft copolymers by forming an intimate mixture of two or more polymers at least one of which includes one or more amino functions, as for example a nylon, and at least one of the remaining polymers includes one or more carboxylic acid functions, as for example a polyester, and a phosphite compound; and thereafter heating the intimate mixture to form the desired block and/or graft copolymers. U.S. Pat. No. 4,417,031 disclose that such copolymers can be spun into fibers.
The use of polyester fibers as the filter element for air filters of air breathing engines is known. For example, the use of such fibers is described in Lamb, George, E. R. et al., "Influence of Fiber Properties on the Performance of Nonwoven Air Fillers," Proc. Air Pollut. Control Assoc., vol. 5, pp. 75-57 (June 15-20; 1975) and Lamb, George E. R. et al. "Influence of Fiber Geometry on the Performance of Non Woven Air Filters," Textile Research Journal," vol. 45 No. 6 pp. 452-463 (1975).
The present invention is directed to a polyester based fiber useful for the filter element of air filters. More particularly, this invention comprises a polymer fiber comprising predominantly one or more melt spinnable polyesters having non uniformly dispersed therein one or more polyolefins; the concentration of said polyolefin at or near the outer surface of said fiber being greater than the concentration of said polyester at or near the surface of the fiber. As used herein, a "fiber" is an elongated body, the length dimension of which is greater than the transverse dimensions of width and thickness. Accordingly, the term fiber includes single filament, ribbon, strip and the like, having regular or irregular cross-section. The fiber of this invention exhibits improved capacity when used as the fibers of the filter element of an air filter.
Yet another aspect of this invention relates to a process of forming the fiber of this invention which comprises melt spinning a molten mixture comprising as a major component one or more melt spinnable polyesters and as a minor component one or more polyolefins forming a polymer fiber comprising predominantly said one or more polyesters having non uniformly dispersed therein said one or more polyolefins, the concentration of said polyolefins being greater at or near the outer surfaces of said fiber being greater than the concentration of said polyesters at or near the center of said fiber. Surprisingly, it has been discovered that during the melt spinning of the fibers, a portion of the polyolefins migrates to the surface of the fiber such that even though it is the minor component, the concentration of the polyolefins at or near the surface of the polyolefins at or near the surface of the fiber is greater than the concentration of polyesters at or near the surface.
FIGS. 1 to 10 are cross-sections of various "Multilobal" fibers for use in this invention.
The fiber of this invention comprises two essential components. The fiber is predominantly a melt processible polyester of "fiber forming molecular weight." As used herein, "fiber forming molecular weight" is a molecular weight at which the polymer can be melt spun into a fiber Such molecular weights are well known to those of skill in the art and may vary widely depending on a number of known factors, including the specific type of polymer. In the preferred embodiments of the invention, the molecular weight of the polyester is at least about 5,000, and in the particularly preferred embodiments the molecular weight of the polyester is from about 8,000 to about 100,000. Amongst these particularly preferred embodiments, most preferred are those embodiments in which the molecular weight of the polyester is from about 15,000 to about 50,000.
Polyester useful in the practice of this invention may vary widely. The type of polyester is not critical and the particular polyester chosen for use in any particular situation will depend essentially on the physical properties and features, i.e., desired in the final filter element Thus, a multiplicity of linear thermoplastic polyesters having wide variations in physical properties are suitable for use in this invention.
The particular polyester chosen for use can be a homo-polyester or a co-polyester, or mixtures thereof as desired. Polyesters are normally prepared by the condensation of an organic dicarboxylic acid and an organic diol, and, therefore illustrative examples of useful polyesters will be described hereinbelow in terms of these diol and dicarboxylic acid precursors.
Polyesters which are suitable for use in this invention are those which are derived from the condensation of aromatic, cycloaliphatic, and aliphatic diols with aliphatic, aromatic and cycloaliphatic dicarboxylic acids. Illustrative of useful aromatic diols, are those having from about 6 to about 12 carbon atoms. Such aromatic diols include bis-(p-hydroxyphenyl) ether; bis-(p-hydroxyphenyl) thioether; (bis-(p-hydroxyphenyl)-sulphone; bis-(p-hydroxyphenyl)-methane; 1,2-(bis-(p-hydroxyphenyl)-ethane; 1-phenyl-(p-hydroxyphenyl)-methane; diphenyl-bis(p-hydroxyphenyl)methane; 2,2-bis(4'-hydroxy-3'-dimethylphenyl)propane; 1,1- bis(p-hydroxyphenyl)-butane; 2,2-(bis(p-hydroxyphenyl)-butane; 1,1-(bis-(p-hydroxyphenyl)cyclopentene; 2,2-(bis-(p-hydroxyphenyl)-propane (bisphenol A); 1,1-(bis-(p-hydroxyphenyl)-cyclohexane (bisphenol C); p-xylene glycol; 2,5 dichloro-p-xylylene glycol; p-xylene-diol; and the like.
Suitable cycloaliphatic diols include those having from about 5 to about 8 carbon atoms. Exemplary of such useful cycloaliphatic diols are 1,4-dihydroxy cyclohexane; 1,4-dihydroxy methylcyclohexane; 1,3-dihydroxycyclopentane; 1,5-dihydroxycycloheptane; 1,5-dihydroxycyclooctane; 1,4-cyclohexane dimethanol; and the like. Polyesters which are derived from aliphatic diols are preferred for use in this invention. Useful and preferred aliphatic and cycloaliphatic diols includes those having from about 2 to about 12 carbon atoms, with those having from about 2 to about 6 carbon atoms being particularly preferred. Illustrative of such preferred diol precursors are propylene glycols; ethylene glycol, pentane diols, hexane diols, butane diols and geometrical isomers thereof. Propylene glycol, ethylene glycol, 1,4-cyclohexane dimethanol, and 1,4-butanediol are particularly preferred as diol precursors of polyesters for use in the conduct of this invention.
Suitable dicarboxylic acids for use as precursors in the preparation of useful polyesters are linear and branched chain saturated aliphatic dicarboxylic acids, aromatic dicarboxylic acids and cycloaliphatic dicarboxylic acids. Illustrative of aliphatic dicarboxylic acids which can be used in this invention are those having from about 2 to about 50 carbon atoms, as for example, oxalic acid, malonic acids, dimethyl-malonic acid, succinic acid, octadecylsuccinic acid, pimelic acid, adipic acid, trimethyladipic acid, sebacic acid, suberic acid, azelaic acid and dimeric acids (dimerisation products of unsaturated aliphatic carboxylic acids such as oleic acid) and alkylated malonic and succinic acids, such as octadecylsuccinic acid, and the like.
Illustrative of suitable cycloaliphatic dicarboxylic acids are those having from about 6 to about 15 carbon atoms. Such useful cycloaliphatic dicarboxylic acids include 1,3-cyclobutanedicarboxylic acid, 1,2-cyclopentanedicarboxylic acid, 1,3- and 1,4-cyclohexanedicarboxylic acid, 1,3- and 1,4-dicarboxymethylcyclohexane and 4,4'-dicyclohexydicarboxylic acid, and the like.
Polyester compounds prepared from the condensation of a diol and an aromatic dicarboxylic acid are preferred for use in this invention. Illustrative of such useful aromatic carboxylic acids are terephthalic acid, isophthalic acid and a o-phthalic acid, 1,3-, 1,4-, 2,6 or 2,7-naphthalnedicarboxylic acid, 4,4'-diphenyldicarboxylic acid, 4,4'-diphenylsulphone-dicarboxylic acid, 1,1,3-trimethyl-5-carboxy-3-(p-carboxyphenyl)-indane, diphenyl ether 4,4'-dicarboxylic acid bis-p(carboxyphenyl)methane and the like. Of the aforementioned aromatic dicarboxylic acids, those based on a benzene ring such as terephthalic acid, isophthalic acid, and ortho-phthalic acid are preferred for use and amongst these preferred acid precursors, terephthalic acid is particularly preferred.
In the most preferred embodiments of this invention, poly(ethylene terephthalate), poly(butylene terephthalate), and poly(1,4-cyclohexane dimethylene terephthalate), are the polyesters of choice. Among these polyesters of choice, poly(ethylene terephthalate is most preferred.
The amount of polyester included in the fiber of this invention may vary widely In general, the amount of polyester will vary from about 99.5 to about 75 percent by weight based on the total weight of the fiber. In the preferred embodiments of the invention the amount of polyester in the fiber may vary from about 99 to about 85 percent by weight based on the total weight of the fiber, and in the particularly perferred embodiments of the invention the amount of polyester in the fiber may vary from about 90 to about 98 weight percent on the aforementioned basis. Amongst these partcularly preferred embodiments, most preferred are those embodiments in which the amount of polyester in the fiber is from about 92 to about 95 weight percent based on the total weight of the fiber.
As a second essential component, the fiber of this invention includes one or more polyolefins. The molecular weight of the polyolefin may vary widely. For example, the polyolefin may be a wax having a relatively low molecuar weight i.e., 500 to 1,000 or more. The polyolefin may also be melt spinnable and of fiber forming molecular weight. Such polyolefins for use in the practice of this invention are well known. Usually, the polyolefin is of fiber forming molecular weight having a molecular weight of at least about 5,000. In the preferred embodiments of the invention the molecular weight of the polyolefins is from about 8,000 to about 1,000,000 and in the particularly preferred embodiments is from about 25,000 to about 750,000. Amongst the particularly preferred embodiments most preferred are those in which the molecular weight of the polyolefins is from about 50,000 to about 500,000. Illustrative of polyolefins for use in the practice of this invention are those formed by the polymerization of olefins of the formula:
R1 R2 CH=CH2
R1 and R2 are the same or different and are hydrogen or substituted or unsubstituted alkylphenyl, phenylalkyl, phenyl, or alkyl. Useful polyolefins include polystyrene, polyethylene, polypropylene, polyl(1-octadecene), polyisobutylene, poly(1-pentene), poly(2-methylstyrene), poly(4-methylstyrene), poly(1-hexene), poly(5-methyl-1-hexene), poly(4-methylpentene), poly(1-butene), poly(3-methyl-1-butene), poly(3-phenyl-1-propene), polybutylene, poly(methyl pentene-1), poly(1-hexene), poly(5-methyl-1-hexene), poly(1-octadecene), poly(vinyl cyclopentane), poly(vinylcyclohexane), poly(a-vinylnaphthalene), and the like.
Preferred for use in the practice of this invention are polyolefins of the above referenced formula in which R is hydrogen or alkyl having from 1 to about 12 carbon atoms such as polyethylene, polypropylene, polyisobutylene, poly(4-methyl-1-pentene), poly(1-butene), poly(1-pentene), poly(3-methyl-1-butene), poly(1-hexene), poly(5-methyl-1-hexene), poly(1-octene), and the like.
In the particularly preferred embodiments of this invention, the polyolefins of choice are those in which R1 is hydrogen and R2 is hydrogen or alkyl having from 1 to about 8 carbon atoms such as polyethylene, polypropylene, poly(isobutylene), poly(1-pentene), poly(3-methyl-1-butene), poly(1-hexene), poly(4-methyl-1-pentene), and poly(1-octene). Amongst these particularly preferred embodiments, most preferred are those embodiments in which R1 is hydrogen and R2 is hydrogen or alkyl having from 1 to about 6 carbon atoms such as polyethylene, polypropylene, poly(4-methyl-1-pentene), and polyisobutylene, with polypropylene being the polyolefin of choice.
The amount of polyolefins included in the fiber of the invention may vary widely and is usually from about 0.5 to about 25 percent by weight based on the total weight of the fiber. In the preferred embodiments of this invention, the amount of melt spinnable polyolefins is from about 1 to about 15 weight percent based on the total weight of the fiber; and in the particularly preferred embodiments of the invention the amount of melt spinnable polyolefins in the fiber is from about 2 to about 10 weight percent based on the total weight of the fiber. Amongst the particularly preferred embodiments, most preferred are those embodiments in which the amount of melt spinnable polyolefins is from about 3 to about 8.5 percent by weight based on the total weight of the fiber.
Surprisingly, it has been discovered that in the fiber of this invention the polyolefins are not uniformly dispersed throughout the polyester continuous phase. Rather, the concentration of the melt spinnable polyolefins at or near the surface of the fiber is higher than the concentration of the melt spinnable polyester at or near the surface of the fiber. The result is a fiber which when used in a fiber filter element has a higher capacity and efficiency as compared to polyester fibers which do not contain melt spinnable polyolefins. As used herein "at or near" the surface of the fiber is at least about 50 Å of the fiber surface. In the preferred embodiments of this invention, the weight percent of the polyolefin component in the portion of the fiber forming a sheath about all or a portion of the longitudinal axis of the fiber said sheath having a thickness of at least about 50 Å is at least about 50 weight percent based on the total weight of the sheath. In the particularly preferred embodiments of the invention, the amount of polyolefins contained in said sheath is at least about 80 percent by weight based on the total weight of the sheath, and in the most preferred embodiments the amount of polyolefins contained in the sheath is at least about 85 weight percent to about 98 weight percent being the amount of choice.
Various other optional ingredients, which are normally included in polyester fibers, may be added to the mixture at an appropriate time during the conduct of the process. Normally, these optional ingredients can be added either prior to or after melting of the polyester or polyolefin or a mixture of the polyester and polyolefin Such optional components include fillers, plasticizers, colorants, mold release agents, antioxidants, ultra violet light stabilizers, lubricants, anti-static agents, fire retardants, and the like. These optional components are well known to those of skill in the art, accordingly, only the preferred optional components will be described herein in detal.
While certain cross-sections are preferred for certain uses, in general the cross-sectional shape of the fiber is not critical and can vary widely. The fiber may have an irregular cross section or a regular cross section. For example, the fiber can be flat sheets or ribbons, regular or irregular cylinders, or can have two or more regular or irregular lobes or vanes projecting from the center of axis of the fiber, such fibers are hereinafter referred to as "multilobal" fibers. Illustrative of such multilobal fibers are trilobal, hexalobal, pentalobal, tetralobal, and octalobal filament fibers. In the preferred embodiments of the invention the fibers are filament fibers having a multilobal cross section such that the surface area of the fiber is maximized, such as fibers having the representative cross-sections depicted in FIGS. 1 to 10. Illustrative of such preferred fibers are those fibers which are multilobal and having at least about three projecting lobes, or vanes or projections, and in the particularly preferred embodiments of the invention the fiber is multilobal having at least about five projecting lobes, vanes or projections such as hexalobal or octalobal fibers.
In the preferred embodiments of the invention in which fibers are multilobal, the "modification ratio" of the fiber can affect the effectiveness of the fiber as the filter element of a filter. As used herein, the "modification ratio" is the ratio of the average distance from the tip of the lobes or vanes of the fiber to the longitudinal center of axis of the fiber to the average distance from the base of the lobes or vanes of the fiber to the longitudinal center of axis of the fiber. In general, the greater the modification ratio of the fiber, the greater the effectiveness of the fiber as a filtering element; and conversely, the less the modification ratio of the fiber, the less its effectiveness as a filtering element. In the preferred embodiments of the invention, the modification ratio of the fiber is at least about 18, and in the particularly preferred embodiments of the invention is from about 2 to about 7. Amongst these preferred embodiments, most preferred are those embodiments in which the modification ratio of the fiber is from about 2.2 to about 5.
In the preferred embodiments of this invention, foamed fibers are implied in the fabrication of the filter elements. Such foamed fibers can be prepared by using conventional foaming techniques, as for example U.S. Pat. Nos. 4,562,022, 4,544,594, 4,380,594 and 4,164,603.
The fiber of this invention is prepared by the process of this invention which comprises:
(a) forming a molten mixture comprising as a major amount one or more polyesters of fiber forming molecular weight and as a minor amount of one or more polyolefins; and
(b) melt spinning said mixture to form a fiber which comprises a major amount of a continuous phase comprising said polyesters and a minor amount of said polyolefins non-uniformly dispersed in said continuous phase such that the concentration of said polyolefins at or near the surface of said fiber is greater than the concentration of said polyesters at or near the center of said fiber.
A molten mixture is formed in the first process step. As used herein, "molten mixture" is an intimate mixture which has been heated to a temperature which is equal to or greater than the melting point of the highest melting polymer component of the mixture or an intimate mixture formed by melting one polymer and dispersing the other polymer in the melted polymer. The manner in which the molten mixture is formed is not critical and conventional methods can be employed. For example, in the preferred embodiments of the invention, the molten mixture can be formed through use of conventional polymer and additive blending means, in which the polymeric components are heated to a temperature equal to or greater than the melting point of the highest melting polymer, and below the degradation temperature of each of the polymers.
In the preferred embodiment, the components of the intimate mixture can be granulated, and the granulated components mixed dry in a suitable mixer, as for example a tumbler or a Branbury Mixer, or the like, as uniformly as possible. Thereafter, the composition is heated in an extruder until the polymer components are melted.
Fibers can be melt spun from the molten mixture by conventional spinning techniques. For example, the compositions can be melt spun in accordance with the procedures of U.S. Pat. Nos. 4,454,196 and 4,410,473. Foamed fibers can be melt spun using conventional procedures, as for example by the procedures of U.S. Pat. Nos 4,562,022 and 4,164,603.
The fibers produced from the composition of this invention can be employed in the many applications in which synthetic fibers are used, and are particularly suited for use in the fabrication of filter elements of various types of air and liquid filters, such as air and liquid filters for industrial applications as for example filters for internal combustion engines, clarification filters for water and other liquids, compressed air filters, industrial air filters and the like employing conventional techniques. Fibers of this invention exhibit enhanced capacity and efficiency when are used as filter elements, as compared to polyesters which do not include minor amounts of the polyolefin.
The fibers of this invention are also useful in the fabrication of coverstock. For example, such fibers can be used as coverstock for absorbant materials in the manufacture of diapers, incontinence pads and the like.
The following examples are presented to more particularly illustrate the invention and should not be construed as limitations thereon.
Polyethylene terephthalate (PET) received from St. Jude as chopped preforms was granulated into 1/8" (0.3175 cm) to 1/4" (0.635 cm) pieces which were then dried in a Stokes vacuum tray drier at 0.5 mm Hg for 16 hrs. at 160° C. The dry PET was sealed in a jar along with a polyolefin and tumbled for fifteen minutes for uniform blending. The anhydrous mixture was placed in the hopper of a one inch (2.54 cm) diameter MPM extruder which was preheated to the desired temperature profile along the barrel of the extruder to yield a polymer melt temperature at the exit of the extruder of about 540° F. (282° C.). The screw was 1 inch (2.54 cm) in diameter and 30 inches (76.2 cm) long with a 4:1 compression ratio. It had a standard feed screw configuration with a modified mixing section consisting of a four inch (10.2 cm) long cross hatched zone located seven inches (17.8 cm) from the end of the screw. The extruder was equipped with a metering pump and a spinning block containing screens (eight layers, 90, 200, 200, 200, 200, 200, 200, 90 mesh top to bottom) and a spinnerette. The spinnerette had twenty (20) symmetrical hexalobal orifices, wherein each lobe has dimension of 4 mils (0.1 mm) (width) x 25 mils (0.635 mm) (length)×20 mils (0.508 mm) (depth). The polymer mixture was extruded at a rate of 13 g/min. The filaments exiting from the spinnerette orifices were drawn down while being cooled in air to a temperature at which the filaments did not stick to the surface of a first take-up roll. Just above the first take-up roll, a finish was applied to the yarn to aid further processing and to dissipate any static charge buildup. The yarn on the first take-up roll was then drawn in line. The yarn on the first take-up roll which turned at 1670 rpm (2800 ft/sec) (853 m/sec) yarn speed was advanced to a second roll which turned at 4482 rpm (6500 ft/sec) (1981 m/sec) and from a second roll onto a third roll which turned also at 4482 rpm (6500 ft/sec) (1981 m/sec). The yarn was then advanced from the third roll to a Leesona winder at 6500 ft/sec (1981 m/sec), which wound the yarn upon a sleeve. The temperature of the rolls (heated by induction heating) were 120° C., 160° C. and 23° C. for rolls 1, 2 and 3 respectively. The results are set forth in the following Table I.
TABLE I______________________________________ Amount of Amount of wt %Ex. No. PET(g) Polymer(g) Polymer______________________________________I 1900 g 100 g PP1 5% PPII 975 g 25 g PP 2.5% PPIII 925 g 75 g PP 7.5% PPIV 950 g 50 g PMP2 5% PMPV 925 g 75 g PMP 7.5% PMPVI 962.5 g 37.5 g PMP 3.75% PMP______________________________________ 1 "PP" is spinning grade polypropylene obtained from Soltex Corporation under the trade name Soltex 3606. 2 "PMP" is spinning grade polymethylpentene obtained from Mitsui Corporation under the trade name TPX.
Using the procedure of Examples I to VI, 950 g of spinning grade polycaprolactam obtained from Allied Corporation under the trade name Capron® LSB, and 50 grams of spinning grade polypropylene obtained from SOLTEX Corporation under the trade name Soltex® 3606, were mixed and melt spun to obtain a 15 denier fiber containing five percent by weight of polypropylene.
A series of experiments were conducted to illustrate the unique nature of fibers containing polyethylene terephthalate and a polyolefin as compared to fibers containing polycaprolactam and such polymers. The fibers of this invention selected for testing are those of Examples III and IV, and the nylon based fiber selected for testing is that of Comparative Example I. In these experiments, x-ray Photoelectron Spectroscopy (XPS) studies were carried out to determine the distribution of the minor amount of the polyolefin in the fiber Procedure employed was as follows: The above fibers were wrapped around a strip of molybdenum foil in order to provide a support for mounting on the sample holder. After introduction into the analysis chamber of the spectrometer, liquid nitrogen was passed through the sample holder to cool the specimen to a temperature of ca. -70° C. as measured by a thermocouple. The analysis was performed on a PHI Model 560 electron spectrometer using MgK α radiation as the excitation source.
In addition, spectra of the pure PET, PP, nylon and PMP were taken for reference. Calculations of the surface composition were based on fitting of lineshapes of the pure components to the convoluted envelope of the mixture. As a secondary measure of the composition, peaks heights ratios were used for those cases involving PET utilizing the C═0 and C--H peaks for determination of the relative quantity of PET. Agreement between the two methods of calculation was within 10%. Estimates of the sampling depth for the samples are on the order of 50-60 Å. In order to minimize decomposition under X-ray exposure, the samples were cooled to a temperature of ca. -70° C. during analysis.
The results indicated that the distribution of PP was substantially uniform in the fiber containing 5% PP (bulk concentration) of Comparative Example I and no segregation of PP at or near the surface regions of the fiber was not detected. For PET/7.5% PP fibers of Example III, the PP concentration within that portion of the fiber from 50 to 60 Å of the surface was determined to be 95-100% and the concentration of PET within this region was from 5 to 0%. This indicated that in contrast to the nylon/PP fiber of Comparative Example I, the concentration of PP in that region within 60 Å of the surface of the fiber is greater than the concentration of PET within that region, even though the concentration of PET within the fiber as a whole is very much greater than that of PP. Similarly, for PET/5% PMP fibers of Example IV, the concentration in the region within 60 Å of the surface of the fiber was determined to be 85-90%, while concentration of PET in this region was 15-10%. For the present experiments, it was not possible to determine if the PP or PMP distribution is homogeneous throughout the analysis volume or if a concentration gradient existed.
A series of experiments were carried out to compare the efficacy of the fibers of this invention as filter mediums to the efficacy of polyester alone for such use. Filter media used in these experiments were fabricated as follows:
The experimental fibers were crimped or texturized and cut into staple length of approximately 11/2 inch (3.81 cm). The fibers were pre-opened on a roller top card and blended with 3DPF 11/4 inch (3.17 cm) staple crimped Vinyon Fibers (a copolymer binding fiber comprising 85% polyvinyl chloride 15% polyvinyl acetate). The blend comprising 2/3 by weight of the experimental fiber or control fiber and 1/3 by weight of the binder fiber. A 6 ounce/yd2 (0.02g/cm2) air laid batting was made on a 12 inch wide laboratory air laying machine known as a Rando Webber. The air laid batting was needle locked on a needle punching machine. The needle locked batting was then needle punched to a spun bonded material known as DuPont's Reemay® 2470, a 3 ounce/yd2 (0.01g/cm2) fabric. Two control fibers were employed: (1) A 3,DPF trilobal cross section DuPont Dacron® Polyester Fiber (crimped, 11/2 inch (3.81 cm) staple length) and (2) and experimental 3DPF 100% polyester 3 DPF hexalobal cross section fiber crimped or texturized and cut into a 11/2 inch (3.81 cm) staple length. Both the unbacked needle locked air laid batting, and the reemay backed batting were heat stabilized for 5 minutes at 275° F. (135° C.) in a mechanical convection oven prior to flat sheet filtration performance testing.
After fabrications the filter mediums were evaluated. The properties selected for evaluation were capacity and efficiency because these properties are ultimately determinative of the effectiveness of a filter medium. The procedure employed is as follows:
On a flat sheet test apparatus, a 61/2"×61/2" (16.5 cm×16.5 cm) specimen was clamped A 4×4 (10.16 cm×10.16 cm) mesh screen was used to support the unbacked test specimen; no screen was used to support the Reemay® backed test specimen. A six inch (15.24 cm) diameter circle of the test specimen was subjected to an air flow of 25 CFM AC dust fine or coarse (1.0 g/in) was interspersed into the air stream by a feeder-aspirator mechanism. Air flow was straigtened by a horn to produce uniform air flow velocity or laminar flow through the specimen. A tared absolute filter consisting of a micro glass phenolic bonded batting classified as AF 31/2 inch (8.9 cm) by the fiber glass insulation industry, 10 inches (25.4 cm) in diameter below the test specimen was used for determining AC dust removal efficiency. The backed specimens were run until a 10 inch (25.4 cm) of water rise in pressure differential across the specimen is reached.
The test contaminant was a natural siliceous granular powder obtained from the Arizona desert classified to a specific particle size distribution and marketed by the AC Spark Plug Division of General Motors. The particle size distributions of the two test dusts are set forth in the following Table II.
TABLE II______________________________________AC Fine AC CoarseParticle ParticleSize (μm) % Size (μm) %______________________________________5.5 <38 ± 3 5.5 <13 ± 311 <54 ± 3 11 <24 ± 322 <71 ± 3 22 <37 ± 344 <89 ± 3 44 <56 ± 388 -- 88 <84 ± 3176 <100 176 <100______________________________________
Dust Removal efficiency of fine and coarse particles was determined by obtaining the weight increase of both the test specimen and the absolute filter: ##EQU1## Where W1 is the weight increase of the test specimen and W2 is the weight increase of the absolute filter.
Capacity is calculated as follows:
The results of this evaluation are set forth in the following Table III:
TABLE III______________________________________Filter AC Course Test Dust AC Fine Test DustMedium Capacity Efficiency Capacity Efficiency______________________________________Polyester.sup.(1) 12.9 99.3 8.29 99.0Polyester.sup.(2) 9.8 99.0 8.14 98.9Example I 15.34 99.3 8.17 99.0______________________________________ .sup.(1) The Polyester fiber is hexalobal. .sup.(2) The Polyester obtained from duPont Co. under the tradename Dacro ® is trilobal. the tradename Dacron® is trilobal.
A series of experiments were carried out to demonstrate that when a polyamide is substituted for a polyester in this invention, the polyolefin is more uniformly dispersed which results in inferior performance when used as a filter medium. The fiber of this invention used in the comparison study was the trilobal fiber prepared as described in Example I containing polyethylene terephthalate and 5% by weight PP, and the fiber of Comparative Example 1 containing polypoprolactam and 5% by weight PP.
The fibers were fabricated into a filter element and evaluated in accordance with the procedure of Example IV. The results are set forth in the following Table III.
TABLE III______________________________________Filter AC Course Test Dust AC Fine Test DustMedium Capacity Efficiency Capacity Efficiency______________________________________Nylon/PP 10.3 99.3 6.8 98.7Example I 15.34 99.3 8.17 99.0______________________________________
|Patente citada||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US3359344 *||6 Jul 1964||19 Dic 1967||Kurashiki Rayon Co||Mixed spun fibers containing polyamides or polyesters and a second component selected from the group of polyethylene, polypropylene or polystyrene|
|US3425893 *||3 Ago 1965||4 Feb 1969||Sims James G||Textile filaments|
|US3498941 *||22 Ago 1966||3 Mar 1970||Ici Ltd||Polymeric dispersions of a polyolefin with an incompatible polymer and a polyamide dispersing agent|
|US3508390 *||30 Sep 1968||28 Abr 1970||Allied Chem||Modified filament and fabrics produced therefrom|
|US3549734 *||27 Jun 1967||22 Dic 1970||Takeshi Yasuda||Method of forming microfibers|
|US3620892 *||7 May 1968||16 Nov 1971||Allied Chem||Dimensionally stable articles and method of making same|
|US3623939 *||28 Jun 1968||30 Nov 1971||Toray Industries||Crimped synthetic filament having special cross-sectional profile|
|US3900549 *||1 Jun 1973||19 Ago 1975||Kuraray Co||Method of spinning composite filaments|
|US3923726 *||9 Jun 1969||2 Dic 1975||Minnesota Mining & Mfg||Process of making colored high temperature polymers|
|US4424258 *||24 Ene 1983||3 Ene 1984||Monsanto Company||Self-crimping multi-component polyester filament wherein the components contain differing amounts of polyolefin|
|US4609710 *||19 Dic 1983||2 Sep 1986||Teijin Limited||Undrawn polyester yarn and process for manufacturing|
|GB1194704A *||Título no disponible|
|Patente citante||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US5336552||26 Ago 1992||9 Ago 1994||Kimberly-Clark Corporation||Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer|
|US5382400||21 Ago 1992||17 Ene 1995||Kimberly-Clark Corporation||Nonwoven multicomponent polymeric fabric and method for making same|
|US5405682||26 Ago 1992||11 Abr 1995||Kimberly Clark Corporation||Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and elastomeric thermoplastic material|
|US5418045||22 Sep 1994||23 May 1995||Kimberly-Clark Corporation||Nonwoven multicomponent polymeric fabric|
|US5425987||6 Oct 1994||20 Jun 1995||Kimberly-Clark Corporation||Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and elastomeric thermoplastic material|
|US5480710 *||17 Mar 1995||2 Ene 1996||E. I. Du Pont De Nemours And Company||Fiberballs|
|US5628736 *||28 Sep 1995||13 May 1997||The Procter & Gamble Company||Resilient fluid transporting network for use in absorbent articles|
|US5643662||21 Ene 1994||1 Jul 1997||Kimberly-Clark Corporation||Hydrophilic, multicomponent polymeric strands and nonwoven fabrics made therewith|
|US5698322 *||2 Dic 1996||16 Dic 1997||Kimberly-Clark Worldwide, Inc.||Multicomponent fiber|
|US5707735 *||18 Mar 1996||13 Ene 1998||Midkiff; David Grant||Multilobal conjugate fibers and fabrics|
|US5762734 *||30 Ago 1996||9 Jun 1998||Kimberly-Clark Worldwide, Inc.||Process of making fibers|
|US5770531 *||29 Abr 1996||23 Jun 1998||Kimberly--Clark Worldwide, Inc.||Mechanical and internal softening for nonwoven web|
|US5811045 *||25 Feb 1997||22 Sep 1998||Kimberly-Clark Worldwide, Inc.||Process of making multicomponent fibers containing a nucleating agent|
|US5820973 *||22 Nov 1996||13 Oct 1998||Kimberly-Clark Worldwide, Inc.||Heterogeneous surge material for absorbent articles|
|US5843063 *||22 Nov 1996||1 Dic 1998||Kimberly-Clark Worldwide, Inc.||Multifunctional absorbent material and products made therefrom|
|US5853881 *||11 Oct 1996||29 Dic 1998||Kimberly-Clark Worldwide, Inc.||Elastic laminates with improved hysteresis|
|US5874160 *||20 Dic 1996||23 Feb 1999||Kimberly-Clark Worldwide, Inc.||Macrofiber nonwoven bundle|
|US5879343 *||22 Nov 1996||9 Mar 1999||Kimberly-Clark Worldwide, Inc.||Highly efficient surge material for absorbent articles|
|US5883231 *||21 Ago 1997||16 Mar 1999||Kimberly-Clark Worldwide, Inc.||Artificial menses fluid|
|US5910545 *||31 Oct 1997||8 Jun 1999||Kimberly-Clark Worldwide, Inc.||Biodegradable thermoplastic composition|
|US5916678 *||16 Oct 1996||29 Jun 1999||Kimberly-Clark Worldwide, Inc.||Water-degradable multicomponent fibers and nonwovens|
|US5931823 *||31 Mar 1997||3 Ago 1999||Kimberly-Clark Worldwide, Inc.||High permeability liner with improved intake and distribution|
|US5965468 *||31 Oct 1997||12 Oct 1999||Kimberly-Clark Worldwide, Inc.||Direct formed, mixed fiber size nonwoven fabrics|
|US5976694 *||3 Oct 1997||2 Nov 1999||Kimberly-Clark Worldwide, Inc.||Water-sensitive compositions for improved processability|
|US5985450 *||22 Sep 1993||16 Nov 1999||Shakespeare||Striated monofilaments useful in the formation of papermaking belts|
|US5994615 *||16 Dic 1998||30 Nov 1999||Kimberly-Clark Worldwide, Inc.||Highly efficient surge material for absorbent article|
|US6040255 *||25 Jun 1996||21 Mar 2000||Kimberly-Clark Worldwide, Inc.||Photostabilization package usable in nonwoven fabrics and nonwoven fabrics containing same|
|US6098557 *||23 Jun 1999||8 Ago 2000||Kimberly-Clark Worldwide, Inc.||High speed method for producing pant-like garments|
|US6121170 *||17 Jun 1999||19 Sep 2000||Kimberly-Clark Worldwide, Inc.||Water-sensitive compositions for improved processability|
|US6152904 *||22 Nov 1996||28 Nov 2000||Kimberly-Clark Worldwide, Inc.||Absorbent articles with controllable fill patterns|
|US6172276||25 Mar 1998||9 Ene 2001||Kimberly-Clark Worldwide, Inc.||Stabilized absorbent material for improved distribution performance with visco-elastic fluids|
|US6187437 *||10 Sep 1998||13 Feb 2001||Celanese Acetate Llc||Process for making high denier multilobal filaments of thermotropic liquid crystalline polymers and compositions thereof|
|US6194483||9 Nov 1999||27 Feb 2001||Kimberly-Clark Worldwide, Inc.||Disposable articles having biodegradable nonwovens with improved fluid management properties|
|US6195975||8 Jun 1999||6 Mar 2001||Belmont Textile Machinery Co., Inc.||Fluid-jet false-twisting method and product|
|US6197860||9 Nov 1999||6 Mar 2001||Kimberly-Clark Worldwide, Inc.||Biodegradable nonwovens with improved fluid management properties|
|US6201068||9 Nov 1999||13 Mar 2001||Kimberly-Clark Worldwide, Inc.||Biodegradable polylactide nonwovens with improved fluid management properties|
|US6203905||30 Ago 1995||20 Mar 2001||Kimberly-Clark Worldwide, Inc.||Crimped conjugate fibers containing a nucleating agent|
|US6207755||11 Ago 1999||27 Mar 2001||Kimberly-Clark Worldwide, Inc.||Biodegradable thermoplastic composition|
|US6211294||29 Dic 1998||3 Abr 2001||Fu-Jya Tsai||Multicomponent fiber prepared from a thermoplastic composition|
|US6245831||29 Jun 2000||12 Jun 2001||Kimberly-Clark Worldwide, Inc.||Disposable articles having biodegradable nonwovens with improved fluid management properties|
|US6268434||9 Nov 1999||31 Jul 2001||Kimberly Clark Worldwide, Inc.||Biodegradable polylactide nonwovens with improved fluid management properties|
|US6281407||28 May 1999||28 Ago 2001||Kimberly-Clark Worldwide, Inc.||Personal care product containing a product agent|
|US6306782||25 Ago 1999||23 Oct 2001||Kimberly-Clark Worldwide, Inc.||Disposable absorbent product having biodisintegratable nonwovens with improved fluid management properties|
|US6309377 *||8 Feb 1999||30 Oct 2001||Chisso Corporation||Non-woven fabric and an absorbent article using thereof|
|US6309988||25 Ago 1999||30 Oct 2001||Kimberly-Clark Worldwide, Inc.||Biodisintegratable nonwovens with improved fluid management properties|
|US6348253||9 Feb 2000||19 Feb 2002||Kimberly-Clark Worldwide, Inc.||Sanitary pad for variable flow management|
|US6350399||22 Dic 1999||26 Feb 2002||Kimberly-Clark Worldwide, Inc.||Method of forming a treated fiber and a treated fiber formed therefrom|
|US6352772 *||20 Ago 1999||5 Mar 2002||Shakespeare||Papermaking belts comprising striated monofilaments|
|US6379564||8 May 2000||30 Abr 2002||Ronald Paul Rohrbach||Multi-stage fluid filter, and methods of making and using same|
|US6384297||3 Abr 1999||7 May 2002||Kimberly-Clark Worldwide, Inc.||Water dispersible pantiliner|
|US6398039||24 Oct 1997||4 Jun 2002||Alliedsignal Inc.||High efficient acid-gas-removing wicking fiber filters|
|US6440611||20 Jul 2000||27 Ago 2002||Honeywell International Inc.||Microcapillary battery separator including hollow fibers, and storage battery incorporating same|
|US6441267||5 Abr 1999||27 Ago 2002||Fiber Innovation Technology||Heat bondable biodegradable fiber|
|US6444312||8 Dic 1999||3 Sep 2002||Fiber Innovation Technology, Inc.||Splittable multicomponent fibers containing a polyacrylonitrile polymer component|
|US6454749||11 Ago 1998||24 Sep 2002||Kimberly-Clark Worldwide, Inc.||Personal care products with dynamic air flow|
|US6461457||14 Abr 2000||8 Oct 2002||Kimberly-Clark Worldwide, Inc.||Dimensionally stable, breathable, stretch-thinned, elastic films|
|US6461729||10 Ago 1999||8 Oct 2002||Fiber Innovation Technology, Inc.||Splittable multicomponent polyolefin fibers|
|US6465712||3 Ago 2000||15 Oct 2002||Kimberly-Clark Worldwide, Inc.||Absorbent articles with controllable fill patterns|
|US6468255||31 Ago 2000||22 Oct 2002||Kimberly-Clark Worldwide, Inc.||Front/back separation barrier|
|US6475418||29 Jun 2000||5 Nov 2002||Kimberly-Clark Worldwide, Inc.||Methods for making a thermoplastic composition and fibers including same|
|US6475618||21 Mar 2001||5 Nov 2002||Kimberly-Clark Worldwide, Inc.||Compositions for enhanced thermal bonding|
|US6479154||25 Oct 2000||12 Nov 2002||Kimberly-Clark Worldwide, Inc.||Coextruded, elastomeric breathable films, process for making same and articles made therefrom|
|US6482194||23 Dic 1999||19 Nov 2002||Kimberly-Clark Worldwide, Inc.||Pocket design for absorbent article|
|US6488670||27 Oct 2000||3 Dic 2002||Kimberly-Clark Worldwide, Inc.||Corrugated absorbent system for hygienic products|
|US6495080||28 Jun 2000||17 Dic 2002||Kimberly-Clark Worldwide, Inc.||Methods for making water-sensitive compositions for improved processability and fibers including same|
|US6500538||16 May 1995||31 Dic 2002||Kimberly-Clark Worldwide, Inc.||Polymeric strands including a propylene polymer composition and nonwoven fabric and articles made therewith|
|US6500897||29 Dic 2000||31 Dic 2002||Kimberly-Clark Worldwide, Inc.||Modified biodegradable compositions and a reactive-extrusion process to make the same|
|US6506456||28 Sep 2000||14 Ene 2003||Kimberly-Clark Worldwide, Inc.||Method for application of a fluid on a substrate formed as a film or web|
|US6509092||5 Abr 1999||21 Ene 2003||Fiber Innovation Technology||Heat bondable biodegradable fibers with enhanced adhesion|
|US6534149||9 Feb 2000||18 Mar 2003||Kimberly-Clark Worldwide, Inc.||Intake/distribution material for personal care products|
|US6544455||1 Ago 2000||8 Abr 2003||Kimberly-Clark Worldwide, Inc.||Methods for making a biodegradable thermoplastic composition|
|US6552124||29 Dic 2000||22 Abr 2003||Kimberly-Clark Worldwide, Inc.||Method of making a polymer blend composition by reactive extrusion|
|US6579934||29 Dic 2000||17 Jun 2003||Kimberly-Clark Worldwide, Inc.||Reactive extrusion process for making modifiied biodegradable compositions|
|US6583075||8 Dic 1999||24 Jun 2003||Fiber Innovation Technology, Inc.||Dissociable multicomponent fibers containing a polyacrylonitrile polymer component|
|US6608236||5 May 1998||19 Ago 2003||Kimberly-Clark Worldwide, Inc.||Stabilized absorbent material and systems for personal care products having controlled placement of visco-elastic fluids|
|US6610395||11 Jun 2001||26 Ago 2003||Honeywell International Inc.||Breathable electromagnetic shielding material|
|US6610903||4 Nov 1999||26 Ago 2003||Kimberly-Clark Worldwide, Inc.||Materials for fluid management in personal care products|
|US6613028||22 Dic 1998||2 Sep 2003||Kimberly-Clark Worldwide, Inc.||Transfer delay for increased access fluff capacity|
|US6613029||28 Abr 1999||2 Sep 2003||Kimberly-Clark Worldwide, Inc.||Vapor swept diaper|
|US6613704 *||12 Oct 2000||2 Sep 2003||Kimberly-Clark Worldwide, Inc.||Continuous filament composite nonwoven webs|
|US6617490||6 Oct 2000||9 Sep 2003||Kimberly-Clark Worldwide, Inc.||Absorbent articles with molded cellulosic webs|
|US6632205||25 Ago 2000||14 Oct 2003||Kimberly-Clark Worldwide, Inc.||Structure forming a support channel adjacent a gluteal fold|
|US6642429||26 Jun 2000||4 Nov 2003||Kimberly-Clark Worldwide, Inc.||Personal care articles with reduced polymer fibers|
|US6653524||4 Dic 2000||25 Nov 2003||Kimberly-Clark Worldwide, Inc.||Nonwoven materials with time release additives|
|US6692603||6 Oct 2000||17 Feb 2004||Kimberly-Clark Worldwide, Inc.||Method of making molded cellulosic webs for use in absorbent articles|
|US6706092||17 Abr 2002||16 Mar 2004||Alliedsignal Inc.||Chemical/Biological decontamination filter|
|US6709254||17 Oct 2001||23 Mar 2004||Kimberly-Clark Worldwide, Inc.||Tiltable web former support|
|US6709623||1 Nov 2001||23 Mar 2004||Kimberly-Clark Worldwide, Inc.||Process of and apparatus for making a nonwoven web|
|US6752905||8 Oct 2002||22 Jun 2004||Kimberly-Clark Worldwide, Inc.||Tissue products having reduced slough|
|US6759567||27 Jun 2001||6 Jul 2004||Kimberly-Clark Worldwide, Inc.||Pulp and synthetic fiber absorbent composites for personal care products|
|US6765125||12 Feb 1999||20 Jul 2004||Kimberly-Clark Worldwide, Inc.||Distribution—Retention material for personal care products|
|US6767498||6 Oct 1999||27 Jul 2004||Hills, Inc.||Process of making microfilaments|
|US6777056||12 Oct 2000||17 Ago 2004||Kimberly-Clark Worldwide, Inc.||Regionally distinct nonwoven webs|
|US6777496||7 Feb 2001||17 Ago 2004||Honeywell International Inc.||Polymeric additives and polymeric articles comprising said additive|
|US6780357||8 Nov 2002||24 Ago 2004||Fiber Innovation Technology, Inc.||Splittable multicomponent polyester fibers|
|US6783837||1 Oct 1999||31 Ago 2004||Kimberly-Clark Worldwide, Inc.||Fibrous creased fabrics|
|US6787184||5 Dic 2001||7 Sep 2004||Kimberly-Clark Worldwide, Inc.||Treated nonwoven fabrics|
|US6794024||25 Oct 2000||21 Sep 2004||Kimberly-Clark Worldwide, Inc.||Styrenic block copolymer breathable elastomeric films|
|US6797226||9 Oct 2001||28 Sep 2004||Kimberly-Clark Worldwide, Inc.||Process of making microcreped wipers|
|US6815383||24 May 2000||9 Nov 2004||Kimberly-Clark Worldwide, Inc.||Filtration medium with enhanced particle holding characteristics|
|US6838154||9 Dic 1998||4 Ene 2005||Kimberly-Clark Worldwide, Inc.||Creped materials|
|US6838402||21 Sep 1999||4 Ene 2005||Fiber Innovation Technology, Inc.||Splittable multicomponent elastomeric fibers|
|US6838590||27 Jun 2001||4 Ene 2005||Kimberly-Clark Worldwide, Inc.||Pulp fiber absorbent composites for personal care products|
|US6846448||20 Dic 2001||25 Ene 2005||Kimberly-Clark Worldwide, Inc.||Method and apparatus for making on-line stabilized absorbent materials|
|US6861380||6 Nov 2002||1 Mar 2005||Kimberly-Clark Worldwide, Inc.||Tissue products having reduced lint and slough|
|US6869670||31 May 2001||22 Mar 2005||Kimberly-Clark Worldwide, Inc.||Composites material with improved high viscosity fluid intake|
|US6881375||30 Ago 2002||19 Abr 2005||Kimberly-Clark Worldwide, Inc.||Method of forming a 3-dimensional fiber into a web|
|US6887350||13 Dic 2002||3 May 2005||Kimberly-Clark Worldwide, Inc.||Tissue products having enhanced strength|
|US6890989||12 Mar 2001||10 May 2005||Kimberly-Clark Worldwide, Inc.||Water-responsive biodegradable polymer compositions and method of making same|
|US6896843||30 Ago 2002||24 May 2005||Kimberly-Clark Worldwide, Inc.||Method of making a web which is extensible in at least one direction|
|US6897348||28 Dic 2001||24 May 2005||Kimberly Clark Worldwide, Inc||Bandage, methods of producing and using same|
|US6908458||25 Ago 2000||21 Jun 2005||Kimberly-Clark Worldwide, Inc.||Swellable structure having a pleated cover material|
|US6929714||23 Abr 2004||16 Ago 2005||Kimberly-Clark Worldwide, Inc.||Tissue products having reduced slough|
|US6946195||18 Sep 2002||20 Sep 2005||Kimberly-Clark Worldwide, Inc.||Compositions for enhanced thermal bonding|
|US6949288||4 Dic 2003||27 Sep 2005||Fiber Innovation Technology, Inc.||Multicomponent fiber with polyarylene sulfide component|
|US6958103||23 Dic 2002||25 Oct 2005||Kimberly-Clark Worldwide, Inc.||Entangled fabrics containing staple fibers|
|US6967261||28 Dic 2001||22 Nov 2005||Kimberly-Clark Worldwide||Bandage, methods of producing and using same|
|US7018531||27 Ene 2003||28 Mar 2006||Honeywell International Inc.||Additive dispensing cartridge for an oil filter, and oil filter incorporating same|
|US7022201||23 Dic 2002||4 Abr 2006||Kimberly-Clark Worldwide, Inc.||Entangled fabric wipers for oil and grease absorbency|
|US7045029||31 May 2001||16 May 2006||Kimberly-Clark Worldwide, Inc.||Structured material and method of producing the same|
|US7053151||29 Dic 2000||30 May 2006||Kimberly-Clark Worldwide, Inc.||Grafted biodegradable polymer blend compositions|
|US7056580||1 Abr 2004||6 Jun 2006||Fiber Innovation Technology, Inc.||Fibers formed of a biodegradable polymer and having a low friction surface|
|US7118639||31 May 2001||10 Oct 2006||Kimberly-Clark Worldwide, Inc.||Structured material having apertures and method of producing the same|
|US7150616||22 Dic 2003||19 Dic 2006||Kimberly-Clark Worldwide, Inc||Die for producing meltblown multicomponent fibers and meltblown nonwoven fabrics|
|US7182863||8 Jun 2004||27 Feb 2007||Honeywell International, Inc.||Additive dispersing filter and method of making|
|US7194788||23 Dic 2003||27 Mar 2007||Kimberly-Clark Worldwide, Inc.||Soft and bulky composite fabrics|
|US7194789||23 Dic 2003||27 Mar 2007||Kimberly-Clark Worldwide, Inc.||Abraded nonwoven composite fabrics|
|US7198621||19 Dic 2002||3 Abr 2007||Kimberly-Clark Worldwide, Inc.||Attachment assembly for absorbent article|
|US7220478||7 Nov 2003||22 May 2007||Kimberly-Clark Worldwide, Inc.||Microporous breathable elastic films, methods of making same, and limited use or disposable product applications|
|US7270723||13 Ago 2004||18 Sep 2007||Kimberly-Clark Worldwide, Inc.||Microporous breathable elastic film laminates, methods of making same, and limited use or disposable product applications|
|US7291264||30 May 2001||6 Nov 2007||Honeywell International, Inc.||Staged oil filter incorporating additive-releasing particles|
|US7316778||26 Ene 2004||8 Ene 2008||Honeywell International, Inc.||Staged oil filter incorporating pelletized basic conditioner|
|US7320948||20 Dic 2002||22 Ene 2008||Kimberly-Clark Worldwide, Inc.||Extensible laminate having improved stretch properties and method for making same|
|US7488441||20 Dic 2002||10 Feb 2009||Kimberly-Clark Worldwide, Inc.||Use of a pulsating power supply for electrostatic charging of nonwovens|
|US7582178||22 Nov 2006||1 Sep 2009||Kimberly-Clark Worldwide, Inc.||Nonwoven-film composite with latent elasticity|
|US7585382||31 Oct 2006||8 Sep 2009||Kimberly-Clark Worldwide, Inc.||Latent elastic nonwoven composite|
|US7635745||31 Ene 2006||22 Dic 2009||Eastman Chemical Company||Sulfopolyester recovery|
|US7645353||23 Dic 2003||12 Ene 2010||Kimberly-Clark Worldwide, Inc.||Ultrasonically laminated multi-ply fabrics|
|US7648771||31 Dic 2003||19 Ene 2010||Kimberly-Clark Worldwide, Inc.||Thermal stabilization and processing behavior of block copolymer compositions by blending, applications thereof, and methods of making same|
|US7651653||26 Ene 2010||Kimberly-Clark Worldwide, Inc.||Machine and cross-machine direction elastic materials and methods of making same|
|US7655829||29 Jul 2005||2 Feb 2010||Kimberly-Clark Worldwide, Inc.||Absorbent pad with activated carbon ink for odor control|
|US7685649||20 Jun 2005||30 Mar 2010||Kimberly-Clark Worldwide, Inc.||Surgical gown with elastomeric fibrous sleeves|
|US7687143||30 Mar 2010||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US7687681||30 Mar 2010||Kimberly-Clark Worldwide, Inc.||Menses specific absorbent systems|
|US7707655||15 Dic 2006||4 May 2010||Kimberly-Clark Worldwide, Inc.||Self warming mask|
|US7732039||27 Nov 2002||8 Jun 2010||Kimberly-Clark Worldwide, Inc.||Absorbent article with stabilized absorbent structure having non-uniform lateral compression stiffness|
|US7736350||30 Dic 2002||15 Jun 2010||Kimberly-Clark Worldwide, Inc.||Absorbent article with improved containment flaps|
|US7790640||23 Mar 2006||7 Sep 2010||Kimberly-Clark Worldwide, Inc.||Absorbent articles having biodegradable nonwoven webs|
|US7799968||21 Sep 2010||Kimberly-Clark Worldwide, Inc.||Sponge-like pad comprising paper layers and method of manufacture|
|US7803244||31 Ago 2006||28 Sep 2010||Kimberly-Clark Worldwide, Inc.||Nonwoven composite containing an apertured elastic film|
|US7811462||26 Feb 2007||12 Oct 2010||Honeywell International, Inc.||Additive dispersing filter and method of making|
|US7811949||12 Oct 2010||Kimberly-Clark Worldwide, Inc.||Method of treating nonwoven fabrics with non-ionic fluoropolymers|
|US7816285||19 Oct 2010||Kimberly-Clark Worldwide, Inc.||Patterned application of activated carbon ink|
|US7820001||15 Dic 2005||26 Oct 2010||Kimberly-Clark Worldwide, Inc.||Latent elastic laminates and methods of making latent elastic laminates|
|US7833917||16 Nov 2010||Kimberly-Clark Worldwide, Inc.||Extensible and stretch laminates with comparably low cross-machine direction tension and methods of making same|
|US7838447||23 Nov 2010||Kimberly-Clark Worldwide, Inc.||Antimicrobial pre-moistened wipers|
|US7879747||30 Mar 2007||1 Feb 2011||Kimberly-Clark Worldwide, Inc.||Elastic laminates having fragrance releasing properties and methods of making the same|
|US7892993||31 Ene 2006||22 Feb 2011||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US7902094||16 Ago 2005||8 Mar 2011||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US7910795||9 Mar 2007||22 Mar 2011||Kimberly-Clark Worldwide, Inc.||Absorbent article containing a crosslinked elastic film|
|US7923391||12 Abr 2011||Kimberly-Clark Worldwide, Inc.||Nonwoven web material containing crosslinked elastic component formed from a pentablock copolymer|
|US7923392||16 Oct 2007||12 Abr 2011||Kimberly-Clark Worldwide, Inc.||Crosslinked elastic material formed from a branched block copolymer|
|US7923505||13 Nov 2007||12 Abr 2011||Kimberly-Clark Worldwide, Inc.||High-viscosity elastomeric adhesive composition|
|US7931817||26 Abr 2011||Honeywell International Inc.||Additive dispensing device and a thermally activated additive dispensing filter having the additive dispensing device|
|US7931944||25 Nov 2003||26 Abr 2011||Kimberly-Clark Worldwide, Inc.||Method of treating substrates with ionic fluoropolymers|
|US7932196||26 Abr 2011||Kimberly-Clark Worldwide, Inc.||Microporous stretch thinned film/nonwoven laminates and limited use or disposable product applications|
|US7938921||10 May 2011||Kimberly-Clark Worldwide, Inc.||Strand composite having latent elasticity|
|US7943813||30 Dic 2002||17 May 2011||Kimberly-Clark Worldwide, Inc.||Absorbent products with enhanced rewet, intake, and stain masking performance|
|US7994079||9 Ago 2011||Kimberly-Clark Worldwide, Inc.||Meltblown scrubbing product|
|US8003553||30 Oct 2006||23 Ago 2011||Kimberly-Clark Worldwide, Inc.||Elastic-powered shrink laminate|
|US8007904||12 Ene 2009||30 Ago 2011||Fiber Innovation Technology, Inc.||Metal-coated fiber|
|US8017534||13 Sep 2011||Kimberly-Clark Worldwide, Inc.||Fibrous nonwoven structure having improved physical characteristics and method of preparing|
|US8043984||25 Oct 2011||Kimberly-Clark Worldwide, Inc.||Single sided stretch bonded laminates, and methods of making same|
|US8066956||15 Dic 2006||29 Nov 2011||Kimberly-Clark Worldwide, Inc.||Delivery of an odor control agent through the use of a presaturated wipe|
|US8137811||8 Sep 2008||20 Mar 2012||Intellectual Product Protection, Llc||Multicomponent taggant fibers and method|
|US8148278||30 Dic 2010||3 Abr 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8158244||22 Dic 2010||17 Abr 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8163385||22 Dic 2010||24 Abr 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8178199||15 May 2012||Eastman Chemical Company||Nonwovens produced from multicomponent fibers|
|US8187697||30 Abr 2007||29 May 2012||Kimberly-Clark Worldwide, Inc.||Cooling product|
|US8216203||10 Jul 2012||Kimberly-Clark Worldwide, Inc.||Progressively functional stretch garments|
|US8216953||13 Dic 2010||10 Jul 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8227362||13 Dic 2010||24 Jul 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8236713||7 Ago 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8247335||21 Ago 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8257628||4 Sep 2012||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8262958||11 Sep 2012||Eastman Chemical Company||Process of making woven articles comprising water-dispersible multicomponent fibers|
|US8273068||25 Sep 2012||Dow Global Technologies Llc||Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates|
|US8273451||25 Sep 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8277706||2 Oct 2012||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8287510||26 Jul 2010||16 Oct 2012||Kimberly-Clark Worldwide, Inc.||Patterned application of activated carbon ink|
|US8287677||16 Oct 2012||Kimberly-Clark Worldwide, Inc.||Printable elastic composite|
|US8314041||22 Dic 2010||20 Nov 2012||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8324445||30 Jun 2008||4 Dic 2012||Kimberly-Clark Worldwide, Inc.||Collection pouches in absorbent articles|
|US8336115||16 Feb 2010||25 Dic 2012||Kimberly-Clark Worldwide, Inc.||Surgical gown with elastomeric fibrous sleeves|
|US8349963||16 Oct 2007||8 Ene 2013||Kimberly-Clark Worldwide, Inc.||Crosslinked elastic material formed from a linear block copolymer|
|US8361913||29 Ene 2013||Kimberly-Clark Worldwide, Inc.||Nonwoven composite containing an apertured elastic film|
|US8377027||19 Feb 2013||Kimberly-Clark Worldwide, Inc.||Waist elastic members for use in absorbent articles|
|US8387497||5 Mar 2013||Kimberly-Clark Worldwide, Inc.||Extensible absorbent layer and absorbent article|
|US8388877||5 Mar 2013||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8398907||22 Dic 2010||19 Mar 2013||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8399368||19 Mar 2013||Kimberly-Clark Worldwide, Inc.||Nonwoven web material containing a crosslinked elastic component formed from a linear block copolymer|
|US8435908||13 Dic 2010||7 May 2013||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8444895||21 May 2013||Eastman Chemical Company||Processes for making water-dispersible and multicomponent fibers from sulfopolyesters|
|US8444896||21 May 2013||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8475878||14 Oct 2008||2 Jul 2013||Dow Global Technologies Llc||Polyolefin dispersion technology used for porous substrates|
|US8486427||11 Feb 2011||16 Jul 2013||Kimberly-Clark Worldwide, Inc.||Wipe for use with a germicidal solution|
|US8512519||22 Abr 2010||20 Ago 2013||Eastman Chemical Company||Sulfopolyesters for paper strength and process|
|US8513147||27 Ago 2008||20 Ago 2013||Eastman Chemical Company||Nonwovens produced from multicomponent fibers|
|US8551895||22 Dic 2010||8 Oct 2013||Kimberly-Clark Worldwide, Inc.||Nonwoven webs having improved barrier properties|
|US8557374||22 Dic 2010||15 Oct 2013||Eastman Chemical Company||Water-dispersible and multicomponent fibers from sulfopolyesters|
|US8623247||13 Dic 2010||7 Ene 2014||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8637130||10 Feb 2012||28 Ene 2014||Kimberly-Clark Worldwide, Inc.||Molded parts containing a polylactic acid composition|
|US8677513||1 Abr 2005||25 Mar 2014||Kimberly-Clark Worldwide, Inc.||Surgical sleeve for glove retention|
|US8691130||22 Dic 2010||8 Abr 2014||Eastman Chemical Company||Process of making water-dispersible multicomponent fibers from sulfopolyesters|
|US8721827||21 Ago 2012||13 May 2014||Dow Global Technologies Llc||Elastic films and laminates|
|US8795561||29 Sep 2010||5 Ago 2014||Milliken & Company||Process of forming a nanofiber non-woven containing particles|
|US8840757||28 Nov 2012||23 Sep 2014||Eastman Chemical Company||Processes to produce short cut microfibers|
|US8840758||28 Nov 2012||23 Sep 2014||Eastman Chemical Company||Processes to produce short cut microfibers|
|US8859481||15 Dic 2005||14 Oct 2014||Kimberly-Clark Worldwide, Inc.||Wiper for use with disinfectants|
|US8871052||28 Nov 2012||28 Oct 2014||Eastman Chemical Company||Processes to produce short cut microfibers|
|US8882963||28 Nov 2012||11 Nov 2014||Eastman Chemical Company||Processes to produce short cut microfibers|
|US8889572||29 Sep 2010||18 Nov 2014||Milliken & Company||Gradient nanofiber non-woven|
|US8895111||14 Mar 2007||25 Nov 2014||Kimberly-Clark Worldwide, Inc.||Substrates having improved ink adhesion and oil crockfastness|
|US8906200||28 Nov 2012||9 Dic 2014||Eastman Chemical Company||Processes to produce short cut microfibers|
|US8936740||13 Ago 2010||20 Ene 2015||Kimberly-Clark Worldwide, Inc.||Modified polylactic acid fibers|
|US8975305||10 Feb 2012||10 Mar 2015||Kimberly-Clark Worldwide, Inc.||Rigid renewable polyester compositions having a high impact strength and tensile elongation|
|US8980964||10 Feb 2012||17 Mar 2015||Kimberly-Clark Worldwide, Inc.||Renewable polyester film having a low modulus and high tensile elongation|
|US9011625||4 Ene 2013||21 Abr 2015||Kimberly-Clark Worldwide, Inc.||Nonwoven composite containing an apertured elastic film|
|US9040598||10 Feb 2012||26 May 2015||Kimberly-Clark Worldwide, Inc.||Renewable polyester compositions having a low density|
|US9162781||31 Jul 2013||20 Oct 2015||Avent, Inc.||Easy-open protective package for aseptic presentation|
|US9175440||18 Sep 2014||3 Nov 2015||Eastman Chemical Company||Processes to produce short-cut microfibers|
|US9273417||14 Oct 2011||1 Mar 2016||Eastman Chemical Company||Wet-Laid process to produce a bound nonwoven article|
|US9303357||10 Abr 2014||5 Abr 2016||Eastman Chemical Company||Paper and nonwoven articles comprising synthetic microfiber binders|
|US20020014447 *||30 May 2001||7 Feb 2002||Rohrbach Ronald Paul||Staged oil filter incorporating additive-releasing particles|
|US20020172316 *||20 Dic 2001||21 Nov 2002||Roberto Matera||Divertor filtering element for a tokamak nuclear fusion reactor; divertor employing the filtering element; and tokamak nuclear fusion reactor employing the divertor|
|US20030022584 *||4 Sep 2002||30 Ene 2003||Latimer Margaret Gwyn||Resilient fluid management materials for personal care products|
|US20030056893 *||31 May 2001||27 Mar 2003||Delucia Mary Lucille||Structured material having apertures and method of producing the same|
|US20030077970 *||31 May 2001||24 Abr 2003||Delucia Mary Lucille||Structured material and method of producing the same|
|US20030082968 *||12 Dic 2002||1 May 2003||Varunesh Sharma||Nonwoven materials having controlled chemical gradients|
|US20030087574 *||23 Ago 2002||8 May 2003||Latimer Margaret Gwyn||Liquid responsive materials and personal care products made therefrom|
|US20030104748 *||3 Dic 2001||5 Jun 2003||Brown Kurtis Lee||Helically crimped, shaped, single polymer fibers and articles made therefrom|
|US20030113507 *||18 Dic 2001||19 Jun 2003||Niemeyer Michael John||Wrapped absorbent structure|
|US20030119406 *||20 Dic 2001||26 Jun 2003||Abuto Francis Paul||Targeted on-line stabilized absorbent structures|
|US20030120180 *||21 Dic 2001||26 Jun 2003||Kimberly-Clark Worldwide, Inc.||Method and apparatus for collecting and testing biological samples|
|US20030124336 *||26 Nov 2002||3 Jul 2003||Keane James M.||Adhesive system for absorbent structures|
|US20030125688 *||26 Nov 2002||3 Jul 2003||Keane James M.||Adhesive system for mechanically post-treated absorbent structures|
|US20030233735 *||20 Dic 2002||25 Dic 2003||Kimberly-Clark Worldwide, Inc.||Use of a pulsating power supply for electrostatic charging of nonwovens|
|US20040005834 *||2 Jul 2002||8 Ene 2004||Peiguang Zhou||Elastomeric adhesive|
|US20040041307 *||30 Ago 2002||4 Mar 2004||Kimberly-Clark Worldwide, Inc.||Method of forming a 3-dimensional fiber into a web|
|US20040041308 *||30 Ago 2002||4 Mar 2004||Kimberly-Clark Worldwide, Inc.||Method of making a web which is extensible in at least one direction|
|US20040065422 *||8 Oct 2002||8 Abr 2004||Kimberly-Clark Worldwide, Inc.||Tissue products having reduced slough|
|US20040087237 *||6 Nov 2002||6 May 2004||Kimberly-Clark Worldwide, Inc.||Tissue products having reduced lint and slough|
|US20040121121 *||23 Dic 2002||24 Jun 2004||Kimberly -Clark Worldwide, Inc.||Entangled fabrics containing an apertured nonwoven web|
|US20040122385 *||23 Dic 2002||24 Jun 2004||Kimberly-Clark Worldwide, Inc.||Absorbent articles including an odor absorbing and/or odor reducing additive|
|US20040122389 *||23 Dic 2002||24 Jun 2004||Mace Tamara Lee||Use of hygroscopic treatments to enhance dryness in an absorbent article|
|US20040122406 *||19 Dic 2002||24 Jun 2004||Moser Julie A||Attachment assembly for absorbent article|
|US20040127868 *||30 Dic 2002||1 Jul 2004||Kimberly-Clark Worldwide, Inc.||Absorbent article with improved leak guards|
|US20040127878 *||30 Dic 2002||1 Jul 2004||Olson Christopher Peter||Surround stretch absorbent garments|
|US20040127881 *||1 Ene 2003||1 Jul 2004||Stevens Robert Alan||Progressively functional stretch garments|
|US20040140048 *||5 Dic 2003||22 Jul 2004||Lindsay Jeffrey Dean||Method of making molded cellulosic webs for use in absorbent articles|
|US20040154970 *||26 Ene 2004||12 Ago 2004||Rohrbach Ronald Paul||Staged oil filter incorporating pelletized basic conditioner|
|US20040202853 *||28 Abr 2004||14 Oct 2004||Patel Kundan M.||Polymeric additives and polymeric articles comprising said additive|
|US20040265577 *||18 Jun 2003||30 Dic 2004||Hironori Goda||Polyester staple fiber and nonwoven fabric comprising same|
|US20040265579 *||1 Abr 2004||30 Dic 2004||Fiber Innovations Technology, Inc.||Fibers formed of a biodegradable polymer and having a low friction surface|
|US20040265583 *||16 Jul 2004||30 Dic 2004||Fiber Innovation Technology, Inc.||Splittable multicomponent polyester fibers|
|US20050027267 *||31 Jul 2003||3 Feb 2005||Van Dyke Wendy Lynn||Absorbent article with improved fit and free liquid intake|
|US20050054779 *||5 Sep 2003||10 Mar 2005||Peiguang Zhou||Stretchable hot-melt adhesive composition with temperature resistance|
|US20050112969 *||25 Nov 2003||26 May 2005||Kimberly-Clark Worldwide, Inc.||Method of treating substrates with ionic fluoropolymers|
|US20050112970 *||25 Nov 2003||26 May 2005||Kimberly-Clark Worldwide, Inc.||Method of treating nonwoven fabrics with non-ionic fluoropolymers|
|US20050123750 *||4 Dic 2003||9 Jun 2005||Fiber Innovation Technology, Inc. And Ticona||Multicomponent fiber with polyarylene sulfide component|
|US20050129914 *||20 Nov 2003||16 Jun 2005||Rim Peter B.||Protective fabrics|
|US20050133151 *||22 Dic 2003||23 Jun 2005||Maldonado Pacheco Jose E.||Extensible and stretch laminates and method of making same|
|US20050136144 *||22 Dic 2003||23 Jun 2005||Kimberly-Clark Worldwide, Inc.||Die for producing meltblown multicomponent fibers and meltblown nonwoven fabrics|
|US20050136766 *||17 Dic 2003||23 Jun 2005||Tanner James J.||Wet-or dry-use biodegradable collecting sheet|
|US20050136777 *||23 Dic 2003||23 Jun 2005||Kimberly-Clark Worldwide, Inc.||Abraded nonwoven composite fabrics|
|US20050148964 *||29 Dic 2003||7 Jul 2005||Chambers Leon E.Jr.||Absorbent structure having profiled stabilization|
|US20050241750 *||30 Abr 2004||3 Nov 2005||Kimberly-Clark Worldwide, Inc.||Method and apparatus for making extensible and stretchable laminates|
|US20060003658 *||30 Jun 2004||5 Ene 2006||Hall Gregory K||Elastic clothlike meltblown materials, articles containing same, and methods of making same|
|US20060047257 *||31 Ago 2004||2 Mar 2006||Maria Raidel||Extensible absorbent core and absorbent article|
|US20060110997 *||24 Nov 2004||25 May 2006||Snowden Hue S||Treated nonwoven fabrics and method of treating nonwoven fabrics|
|US20060130252 *||16 Dic 2004||22 Jun 2006||Kimberly-Clark Worldwide, Inc.||Cleaning device|
|US20060148354 *||30 Dic 2004||6 Jul 2006||Shelley Lindsay C||Extensible and stretch laminates with comparably low cross-machine direction tension and methods of making same|
|US20060247591 *||29 Abr 2005||2 Nov 2006||Kimberly-Clark Worldwide, Inc.||Waist elastic members for use in absorbent articles|
|US20070000006 *||20 Jun 2005||4 Ene 2007||Jordan Joy F||Surgical gown with elastomeric fibrous sleeves|
|US20070000014 *||20 Jun 2005||4 Ene 2007||John Rotella||Surgical gown with a film sleeve for glove retention and wearer protection|
|US20070098986 *||19 Dic 2006||3 May 2007||Teijin Fibers Limited||Process for producing a nonwoven polyester staple fiber fabric|
|US20070128404 *||1 Dic 2006||7 Jun 2007||Invista North America S.Ar.L.||Hexalobal cross-section filaments with three major lobes and three minor lobes|
|US20070130707 *||13 Dic 2005||14 Jun 2007||Kimberly-Clark Worldwide, Inc.||Cleansing device with inclusion|
|US20070130709 *||13 Dic 2005||14 Jun 2007||Kimberly-Clark Worldwide, Inc.||Methods for employing a cleansing device with inclusion|
|US20070135787 *||14 Dic 2005||14 Jun 2007||Maria Raidel||Extensible absorbent layer and absorbent article|
|US20070137767 *||15 Dic 2005||21 Jun 2007||Thomas Oomman P||Latent elastic laminates and methods of making latent elastic laminates|
|US20070141354 *||30 Oct 2006||21 Jun 2007||James Russell Fitts||Elastic-powered shrink laminate|
|US20070142261 *||15 Dic 2005||21 Jun 2007||Clark James W||Wiper for use with disinfectants|
|US20070142801 *||15 Dic 2005||21 Jun 2007||Peiguang Zhou||Oil-resistant elastic attachment adhesive and laminates containing it|
|US20070224903 *||23 Mar 2006||27 Sep 2007||Kimberly-Clark Worldwide, Inc.||Absorbent articles having biodegradable nonwoven webs|
|US20080040906 *||15 Ago 2007||21 Feb 2008||Fiber Innovation Technology, Inc.||Adhesive core chenille yarns and fabrics and materials formed therefrom|
|US20080099407 *||26 Feb 2007||1 May 2008||Derek Eilers||Additive dispersing filter and method of making|
|US20080110465 *||8 Jun 2007||15 May 2008||Welchel Debra N||Respirator with exhalation vents|
|US20080110819 *||5 Nov 2007||15 May 2008||Ronald Paul Rohrbach||Staged oil filter incorporating additive-releasing particles|
|US20080145267 *||15 Dic 2006||19 Jun 2008||Kimberly-Clark Worldwide, Inc.||Delivery of an odor control agent through the use of a presaturated wipe|
|US20080177242 *||14 Ene 2008||24 Jul 2008||Dow Global Technologies Inc.||Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates|
|US20080227356 *||14 Mar 2007||18 Sep 2008||Simon Poruthoor||Substrates having improved ink adhesion and oil crockfastness|
|US20080268216 *||30 Abr 2007||30 Oct 2008||Kimberly-Clark Worldwide, Inc.||Cooling product|
|US20090156079 *||14 Dic 2007||18 Jun 2009||Kimberly-Clark Worldwide, Inc.||Antistatic breathable nonwoven laminate having improved barrier properties|
|US20090181592 *||12 Ene 2009||16 Jul 2009||Fiber Innovation Technology, Inc.||Metal-coated fiber|
|US20090206024 *||15 Feb 2008||20 Ago 2009||Bilski Gerard W||Additive dispensing device and a thermally activated additive dispensing filter having the additive dispensing device|
|US20090233049 *||11 Mar 2008||17 Sep 2009||Kimberly-Clark Worldwide, Inc.||Coform Nonwoven Web Formed from Propylene/Alpha-Olefin Meltblown Fibers|
|US20090233072 *||11 Mar 2009||17 Sep 2009||James Benjamin Harvey||Fibrous nonwoven structure having improved physical characteristics and method of preparing|
|US20090325440 *||31 Dic 2009||Thomas Oomman P||Films and film laminates with relatively high machine direction modulus|
|US20100018641 *||28 Ene 2010||Kimberly-Clark Worldwide, Inc.||Methods of Applying Skin Wellness Agents to a Nonwoven Web Through Electrospinning Nanofibers|
|US20100063208 *||11 Mar 2010||Merchant Timothy P||Multicomponent Taggant Fibers and Method|
|US20100126321 *||29 Ene 2010||27 May 2010||Maria Raidel||Extensible Absorbent Layer and Absorbent Article|
|US20100138975 *||16 Feb 2010||10 Jun 2010||Joy Francine Jordan||Surgical Gown With Elastomeric Fibrous Sleeves|
|US20100227520 *||14 Oct 2008||9 Sep 2010||Dow Global Technologies Inc.||Polyolefin dispersion technology used for porous substrates|
|US20110084032 *||12 Oct 2010||14 Abr 2011||Derek Eilers||Additive dispersing filter and method of making|
|US20150266263 *||22 May 2013||24 Sep 2015||Mitsui Chemicals, Inc.||Nonwoven fabric laminate for foam molding, urethane foam molding composite including said nonwoven fabric laminate, and method for manufacturing non-woven fabric laminates for foam molding|
|USD746439||30 Dic 2013||29 Dic 2015||Kimberly-Clark Worldwide, Inc.||Combination valve and buckle set for disposable respirators|
|USRE39919||18 May 1999||13 Nov 2007||Kimberly Clark Worldwide, Inc.||Heterogeneous surge material for absorbent articles|
|CN101768804B||26 Dic 2008||18 Abr 2012||徐州斯尔克纤维科技股份有限公司||Different shrinkage two-component network composite filament|
|EP2458085A1||25 Ene 2008||30 May 2012||Kimberly-Clark Worldwide, Inc.||Substrates having improved ink adhesion and oil crockfastness|
|EP2812469A4 *||22 Ene 2013||7 Oct 2015||Kimberly Clark Co||Modified polylactic acid fibers|
|WO1998022068A1||21 Nov 1997||28 May 1998||Kimberly-Clark Worldwide, Inc.||Heterogeneous surge material for absorbent articles|
|WO1998036331A1 *||13 Feb 1998||20 Ago 1998||Bmp Europe Ltd.||A cleaning element|
|WO1999056687A1||30 Abr 1999||11 Nov 1999||Kimberly-Clark Worldwide, Inc.||Stabilized absorbent material for personal care products and method for making|
|WO2003003963A2||3 Jul 2002||16 Ene 2003||Kimberly-Clark Worldwide, Inc.||Refastenable absorbent garment|
|WO2004060244A1||23 Dic 2003||22 Jul 2004||Kimberly-Clark Worldwide, Inc.||Absorbent products with enhanced rewet, intake, and stain masking performance|
|WO2004060255A1||3 Nov 2003||22 Jul 2004||Kimberly-Clark Worldwide, Inc.||Use of hygroscopic treatments to enhance dryness in an absorbent article|
|WO2006073557A1||9 Nov 2005||13 Jul 2006||Kimberly-Clark Worldwide, Inc.||Multilayer film structure with higher processability|
|WO2008075233A1||19 Nov 2007||26 Jun 2008||Kimberly-Clark Worldwide, Inc.||Delivery of an odor control agent through the use of a premoistened wipe|
|WO2009022248A2||29 Jul 2008||19 Feb 2009||Kimberly-Clark Worldwide, Inc.||A disposable respirator with exhalation vents|
|WO2009022250A2||29 Jul 2008||19 Feb 2009||Kimberly-Clark Worldwide, Inc.||A disposable respirator|
|WO2009050610A2||4 Sep 2008||23 Abr 2009||Kimberly-Clark Worldwide, Inc.||Crosslinked elastic material formed from a linear block copolymer|
|WO2009077889A1||17 Sep 2008||25 Jun 2009||Kimberly-Clark Worldwide, Inc.||Antistatic breathable nonwoven laminate having improved barrier properties|
|WO2009138887A2||30 Mar 2009||19 Nov 2009||Kimberly-Clark Worldwide, Inc.||Latent elastic composite formed from a multi-layered film|
|WO2010001272A2||14 May 2009||7 Ene 2010||Kimberly-Clark Worldwide, Inc.||Elastic composite formed from multiple laminate structures|
|WO2010001273A2||14 May 2009||7 Ene 2010||Kimberly-Clark Worldwide, Inc.||Elastic composite containing a low strength and lightweight nonwoven facing|
|WO2011047252A1||15 Oct 2010||21 Abr 2011||E. I. Du Pont De Nemours And Company||Monolithic films having zoned breathability|
|WO2011047264A1||15 Oct 2010||21 Abr 2011||E. I. Du Pont De Nemours And Company||Articles having zoned breathability|
|WO2011128790A2||15 Mar 2011||20 Oct 2011||Kimberly-Clark Worldwide, Inc.||Absorbent composite with a resilient coform layer|
|WO2012080867A1||10 Nov 2011||21 Jun 2012||Kimberly-Clark Worldwide, Inc.||Ambulatory enteral feeding system|
|WO2012085712A1||22 Nov 2011||28 Jun 2012||Kimberly-Clark Worldwide, Inc.||Sterilization container with disposable liner|
|WO2013001381A2||21 May 2012||3 Ene 2013||Kimberly-Clark Worldwide, Inc.||Sheet materials having improved softness|
|WO2013064922A1||18 Sep 2012||10 May 2013||Kimberly-Clark Worldwide, Inc.||Drainage kit with built-in disposal bag|
|WO2014159724A1||12 Mar 2014||2 Oct 2014||Fitesa Nonwoven, Inc.||Extensible nonwoven fabric|
|WO2015015364A1||18 Jul 2014||5 Feb 2015||Avent, Inc.||Easy-open protective package for aseptic presentation|
|WO2015015398A1||28 Jul 2014||5 Feb 2015||Avent, Inc.||Dual layer wrap package for aseptic presentation|
|WO2015131054A1||27 Feb 2015||3 Sep 2015||Avent, Inc.||Surfactant treatment for a sterilization wrap with reduced occurrence of wet packs after steam sterilization|
|WO2016032833A1||20 Ago 2015||3 Mar 2016||Avent, Inc.||Moisture management for wound care|
|WO2016100764A1||18 Dic 2015||23 Jun 2016||Earth Renewable Technologies||Extrudable polylactic acid composition and method of making molded articles utilizing the same|
|Clasificación de EE.UU.||428/393, 428/372, 428/400, 428/397, 428/364|
|Clasificación internacional||D01F6/92, D01F8/14|
|Clasificación cooperativa||Y10T428/2913, D01F6/92, Y10T428/2927, D01F8/14, Y10T428/2973, Y10T428/2978, Y10T428/2965|
|Clasificación europea||D01F6/92, D01F8/14|
|17 May 1995||FPAY||Fee payment|
Year of fee payment: 4
|1 Jun 1999||FPAY||Fee payment|
Year of fee payment: 8
|29 May 2003||FPAY||Fee payment|
Year of fee payment: 12
|18 Jun 2003||REMI||Maintenance fee reminder mailed|